The process for new drug approvals and medical devices relies heavily on the quality of documentation submitted to the regulatory authorities, and a high standard of medical writing plays a vital role in ensuring a positive outcome.
Our medical writing training courses will provide delegates with all the tools and techniques necessary to comply with the required standards.
Our expert team of speakers has extensive knowledge and expertise in this specialist area.
Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
5 Jun 2025 - Online webinar
Also on: 1 Oct 2025
Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission.
Presented by Barbara Grossman (bio)
1-2 Jul 2025 - Online webinar
Also on: 20 Nov 2025
How to produce quality regulatory documents including the clinical evaluation report (CER).
8 Apr 2025 - Online webinar
Also on: 8 Oct 2025
This course will provide attendees with fundamental editing skills, enabling them to refine their own research articles or edit the work of other researchers with confidence.
Presented by Alex Evans (bio)
1 Apr 2025 - Online webinar
Also on: 1 Oct 2025
On this course, learn the basics of writing health and medical articles for the layperson.
Presented by Alex Evans (bio)
29 Apr 2025 - Online webinar
Also on: 15 Oct 2025
Explore the intersection between AI and medical communications in this medical writing power hour.
Presented by Alex Evans (bio)
5-6 Jun 2025 - Online webinar
Also on: 25 Sep 2025
Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive, practical medical writing course will benefit participants by enabling them to achieve this standard.
Presented by Cheryl Roberts (bio)